Lack of benefit of CD34(+) cell selected over non-selected peripheral blood stem cell transplantation in multiple myeloma: results of a single centerstudy
N. Morineau et al., Lack of benefit of CD34(+) cell selected over non-selected peripheral blood stem cell transplantation in multiple myeloma: results of a single centerstudy, LEUKEMIA, 14(10), 2000, pp. 1815-1820
In order to determine the clinical impact of CD34(+) cell selected autologo
us transplantation in multiple myeloma (MM), we have performed a retrospect
ive case-controlled analysis comparing 21 MM patients receiving high-dose m
elphalan and autologous transplantation with CD34(+) peripheral blood stem
cells (PBSC) as front-line therapy to 21 control patients receiving unselec
ted products. Case matching was performed using the following criteria: age
and beta 2-microglobulin at diagnosis and disease status at the time of tr
ansplantation. Both cohorts were homogeneous in term of induction treatment
and conditioning regimen. Patients were collected for CD34(+) selection af
ter priming with G-CSF alone. Significantly fewer CD34(+) cells/kg were inf
used to patients in the selected group as compared to patients in the contr
ol group: 2.2 (range 0.5-14.3) vs 9.4 (range 1.1-15) (P < 0.001). The media
n time to neutrophil recovery greater than or equal to 0.05 x 10(9)/l was 1
0 days for the CD34(+) group and 9.5 days for the control group (P = 0.357)
. The median time to platelet recovery greater than or equal to 20 x 10(9)/
l was 9 days for the CD34(+) group and 4.5 days for the control group (P =
0.005). Response rates were comparable in both groups (85.7% in the CD34(+)
group vs 90.4% in the control group). At 3 years, event-free survival (32%
in the CD34(+) group vs 39% in the control group) and overall survival (85
% in the CD34(+) group vs 79% in the control group) were not significantly
different. Finally, use of unselected products dramatically reduced the cos
t of the transplantation procedure. This study shows that CD34(+) cell sele
cted autologous transplantation is more expensive than transplantation with
unselected products and does not improve the clinical outcome of patients
with MM.